His barrier for 2.5 more wk. (B,C) HCEnC-21 (B) and HCEnC-21T (C) were grown to confluence (3,000 cells/cm2) in perfusion chambers and 20 mM lactate was applied to their apical, basolateral or both cell membranes. Facilitated lactate uptake is H+ coupled and was measured indirectly by detecting intracellular pH changes using the BCECF-AM fluorescent dye. Temporal acidification of both HCEnC-21 and HCEnC-21T was observed after lactate pulses to the apical and basolateral membrane. Error bars indicate mean 6 SEM. *, P,0.05. doi:10.1371/CI 1011 site journal.pone.0051427.gCell Doubling Time (CDT)HCEnC-21 and HCEnC-21T cells were plated in 12-well plates at a density of 50,000 cells per well. Medium was changed at day 2. Cells were trypsinized and counted using a Hemocytometer (Hausser Scientific; Horsham, PA), after 2, 3, and 4 days. Cell numbers were determined for duplicate wells per time point. Two to four different passages were independently analyzed per group, and cell type and results were averaged for data analysis.Telomerase-Immortalized Human HDAC-IN-3 web Corneal EndotheliumReal-time and Reverse Transcription (RT) PCRTotal RNA from cell cultures was isolated using the RNeasy kits (Qiagen; Valencia, CA) or TRIzolH (Invitrogen). Reverse transcription was carried out using a commercially available kit according to the manufacturer’s protocol. TaqManH primers for b-2 microglobulin (B2M), hTERT, Na/K ATPase a1 and a3, NHE1, CA2, Aqp1, and NSE were obtained from Applied Biosystems (Foster City, PA). Real-time PCR reactions were set up in triplicate (Probe Fast master mix; Kapa Biosystems; Woburn, MA), and every gene was detected in at least 3 different passages of HCEnC-21 and HCEnC-21T cells, as well as in 2 passages (,6) of 21M primary cells and stromal fibroblasts. PCR was performed in a Mastercycler Realplex2 (Eppendorf; Hamburg, Germany). For data analysis, results were averaged, SEM was calculated, and the comparative Ct method was performed using B2M as the calibrator. Conventional PCR was performed in a MyCycler Thermal cycler (Bio-Rad; Hercules, CA) following the AmpliTaqH 360 DNA Polymerase protocol (Applied Biosystems) using primers specific to MCT1, 22, and 24, AE2, CA12, CFTR, sAC10, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The nucleotide sequences of these primers are 1317923 listed in Table 1. cDNA (1 ml) was added into a 25 ml reaction that underwent 30 cycles of amplification. PCR products (10 ml) were examined on 1.2 agarose gels stained with ethidium bromide. No-template-controls were performed at the reverse transcription and PCR steps and served as negative controls.values were calculated from a minimum of 3 different passages per cell type run in 2 independent experiments.Gel Electrophoresis and Western BlottingBetween 0.5?*106 cells were lysed in 200 ml RIPA buffer containing HALT protease and phosphatase inhibitors (both Thermo ScientificH; Rockfort, IL) for 30 min on ice. Cell lysates were passed 6 times through a 26-gauge needle and centrifuged at 15,0006g and 4uC for 15 min. The supernatant (180 ml) was transferred into a new tube and the BCA assay (Pierce) was used to determine total protein concentration. Equal amounts of protein were loaded on 10 Bis-Tris gels for SDS-PAGE. Proteins were then electrophoretically transferred to a polyvinylidene difluoride membrane (Millipore), and nonspecific binding was blocked by incubation in 5 nonfat milk diluted in tris-buffered saline containing 0.1 Tween-20 (TBST) for 1 hr at room tem.His barrier for 2.5 more wk. (B,C) HCEnC-21 (B) and HCEnC-21T (C) were grown to confluence (3,000 cells/cm2) in perfusion chambers and 20 mM lactate was applied to their apical, basolateral or both cell membranes. Facilitated lactate uptake is H+ coupled and was measured indirectly by detecting intracellular pH changes using the BCECF-AM fluorescent dye. Temporal acidification of both HCEnC-21 and HCEnC-21T was observed after lactate pulses to the apical and basolateral membrane. Error bars indicate mean 6 SEM. *, P,0.05. doi:10.1371/journal.pone.0051427.gCell Doubling Time (CDT)HCEnC-21 and HCEnC-21T cells were plated in 12-well plates at a density of 50,000 cells per well. Medium was changed at day 2. Cells were trypsinized and counted using a Hemocytometer (Hausser Scientific; Horsham, PA), after 2, 3, and 4 days. Cell numbers were determined for duplicate wells per time point. Two to four different passages were independently analyzed per group, and cell type and results were averaged for data analysis.Telomerase-Immortalized Human Corneal EndotheliumReal-time and Reverse Transcription (RT) PCRTotal RNA from cell cultures was isolated using the RNeasy kits (Qiagen; Valencia, CA) or TRIzolH (Invitrogen). Reverse transcription was carried out using a commercially available kit according to the manufacturer’s protocol. TaqManH primers for b-2 microglobulin (B2M), hTERT, Na/K ATPase a1 and a3, NHE1, CA2, Aqp1, and NSE were obtained from Applied Biosystems (Foster City, PA). Real-time PCR reactions were set up in triplicate (Probe Fast master mix; Kapa Biosystems; Woburn, MA), and every gene was detected in at least 3 different passages of HCEnC-21 and HCEnC-21T cells, as well as in 2 passages (,6) of 21M primary cells and stromal fibroblasts. PCR was performed in a Mastercycler Realplex2 (Eppendorf; Hamburg, Germany). For data analysis, results were averaged, SEM was calculated, and the comparative Ct method was performed using B2M as the calibrator. Conventional PCR was performed in a MyCycler Thermal cycler (Bio-Rad; Hercules, CA) following the AmpliTaqH 360 DNA Polymerase protocol (Applied Biosystems) using primers specific to MCT1, 22, and 24, AE2, CA12, CFTR, sAC10, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The nucleotide sequences of these primers are 1317923 listed in Table 1. cDNA (1 ml) was added into a 25 ml reaction that underwent 30 cycles of amplification. PCR products (10 ml) were examined on 1.2 agarose gels stained with ethidium bromide. No-template-controls were performed at the reverse transcription and PCR steps and served as negative controls.values were calculated from a minimum of 3 different passages per cell type run in 2 independent experiments.Gel Electrophoresis and Western BlottingBetween 0.5?*106 cells were lysed in 200 ml RIPA buffer containing HALT protease and phosphatase inhibitors (both Thermo ScientificH; Rockfort, IL) for 30 min on ice. Cell lysates were passed 6 times through a 26-gauge needle and centrifuged at 15,0006g and 4uC for 15 min. The supernatant (180 ml) was transferred into a new tube and the BCA assay (Pierce) was used to determine total protein concentration. Equal amounts of protein were loaded on 10 Bis-Tris gels for SDS-PAGE. Proteins were then electrophoretically transferred to a polyvinylidene difluoride membrane (Millipore), and nonspecific binding was blocked by incubation in 5 nonfat milk diluted in tris-buffered saline containing 0.1 Tween-20 (TBST) for 1 hr at room tem.
